Remote | United States | Project-Based Independent Contractor Compensation: $20-$50 USD/hour, based on specialty, experience, and project requirements Help Shape the Future of AI in Healthcare What if your pharmaceutical expertise could help artificial intelligence better understand regulatory requirements, scien
About the role
Remote | United States | Project-Based Independent Contractor
Compensation: $20-$50 USD/hour, based on specialty, experience, and project requirements
Help Shape the Future of AI in Healthcare
What if your pharmaceutical expertise could help artificial intelligence better understand regulatory requirements, scientific documentation, manufacturing processes, and quality standards?
At Volga Partners , we're connecting experienced pharmaceutical and biotechnology professionals with opportunities to contribute to the development and evaluation of advanced AI models.
We're seeking pharmaceutical regulatory, quality, manufacturing, compliance, and technical development professionals who can apply their industry expertise, scientific judgment, and regulatory knowledge to evaluate AI-generated pharmaceutical content.
This isn't a traditional pharmaceutical position. You won't be manufacturing products, preparing submissions, or managing quality systems. Instead, you'll assess complex scientific and regulatory content, identify technical inaccuracies, evaluate reasoning, and provide structured feedback that improves AI model performance.
Your pharmaceutical expertise is what matters. AI experience is a plus, not a requirement.
Important Note: This is a freelance, task-based role designed for those seeking supplemental income. It’s essential to understand the nature of freelance work—tasks will be assigned as they become available, and work may be irregular or intermittent.
The Opportunity
As a Pharmaceutical Subject Matter Expert (SME) , you'll serve as a subject matter evaluator, helping assess the quality, accuracy, and reasoning of AI-generated pharmaceutical and biotechnology content.
You'll analyze scientific, regulatory, manufacturing, and compliance-related scenarios, identify errors or unsupported conclusions, and provide expert feedback grounded in industry standards, regulatory frameworks, and professional judgment. …
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